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United States · US · US:76138-220_1cee8d76-1f9c-14b4-e063-6294a90afc0e
5298 SUNSCREEN
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerInnovation Specialties
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11761382200260 mL in 1 BOTTLE (76138-220-02)
Annotations
UNII (FDA Substance ID)
G63QQF2NOX
AVOBENZONE
RxCUI 45045
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "G63QQF2NOX",
"rxcui": "45045",
"inchikey": "XNEFYCZVKIDDMS-UHFFFAOYSA-N",
"display_name": "AVOBENZONE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"667dccd6-5047-4beb-b2f0-0b8d8d79aa01": {
"match": "brand_token",
"title": "5298 SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE) LOTION [INNOVATION SPECIALTIES]",
"spl_version": "3",
"published_date": "2024-07-12"
}
},
"productid": "76138-220_1cee8d76-1f9c-14b4-e063-6294a90afc0e",
"productndc": "76138-220",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
"proprietary_name": "5298 SUNSCREEN",
"active_ingred_unit": "mg/mL; mg/mL; mg/mL; mg/mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Avobenzone, Homosalate, Octocrylene, Octisalate",
"start_marketing_date": "20220510",
"active_numerator_strength": "30; 100; 50; 100"
}Access this data programmatically
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